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  1. FDA Recalls
  2. ›Device Recalls

FDA Device Recalls

Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 4181–4200 of 39,430 recalls

Class IIOngoing

CircuitGuard Bacterial/Viral Filter with Elbow (Model/Catalogue number: SK200FPE / 7056)

Kung Shin Plastics Co. Ltd.

The machine side connector of the filter HME may be occluded by plastic which prevents proper airflow. The issue may lead to ventilation bag malfunction in which the user is unable to inflate/deflate properly during manual ventilation. Potential risks to health include oxygen deprivation, leading to respiratory distress and medical complications.

January 9, 2025 · DeviceView details →
Class IIOngoing

Medline Convenience Kits for Various Procedures: 1) ADULT INTUBATION TRAY, Model Number DYNJAA254A; 2) ADULT MAIN DISP. INTUB PART A, Model Number DYNJAA262A

MEDLINE INDUSTRIES, LP - Northfield

Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.

January 9, 2025 · Device
View details →
Class IIOngoing

CircuitGuard ThermoFlo Filter -Combined Heat and Moisture Exchanger, Bacterial Viral Filter w O2 Port and Elbow (Model/Catalogue number: SK200CPE / 6126)

Kung Shin Plastics Co. Ltd.

The machine side connector of the filter HME may be occluded by plastic which prevents proper airflow. The issue may lead to ventilation bag malfunction in which the user is unable to inflate/deflate properly during manual ventilation. Potential risks to health include oxygen deprivation, leading to respiratory distress and medical complications.

January 9, 2025 · DeviceView details →
Class IIOngoing

A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.

Medtronic Neuromodulation

Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.

January 9, 2025 · DeviceView details →
Class IIOngoing

Medline Convenience Kits for Various Procedures: 1) CLOVIS RESP/INTUB DRAWER 2, Model Number ACC010809; 2) RESP/INTUBATION DRAWER #2, Model Number ACC010813

MEDLINE INDUSTRIES, LP - Northfield

Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.

January 9, 2025 · DeviceView details →
Class IIOngoing

The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of the Rapid fFN Specimen Collection kit (PN: 71738-001). The Collection Tube (PN: 71550-001) is manufactured by a third-party supplier, MML Diagnostics Packaging, and includes the transport tube, cap, and extraction buffer. Tubes are packaged into PN: 71738-00 at Hologic prior to kit release.

Hologic, Inc.

Three lots of Rapid fFN Specimen Collection kit (901164, 901165, and 904850) contain Rapid fFN Specimen Collection Tubes which may be empty, underfilled, or overfilled with extraction buffer. The transport tubes are used with the Fetal Fibronectin Enzyme Immunoassay and Rapid fFN¿ for the TLiIQ¿ System which aids in assessing the risk of preterm delivery. The use of empty transport tubes or transport tubes containing insufficient extraction buffer volume may result in invalid results and/or delays in obtaining results. Additionally, the use of underfilled tubes may result in false positive results and the use of overfilled tubes may result in false negative results.

January 8, 2025 · DeviceView details →
Class IIOngoing

stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades

Stryker Corporation

Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.

January 8, 2025 · DeviceView details →
Class IIOngoing

(1) Pyxis MedStation ES, Catalog No. 323; (2) Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) Pyxis MedStation ES Tower, Catalog No. 352; (4) BD Pyxis CII Safe ES, Catalog No. 1116-00

CareFusion 303, Inc.

Software issues could potentially result in: 1) delays in accessing dispensing software application, 2) wrong therapy (dose, item, timing, etc.), or 3) unauthorized access and/or compliance related issues

January 8, 2025 · DeviceView details →
Class IIOngoing

138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 138911-01 BD PYXIS MEDBANK MINI CR-4HH-P 169-115 BD PYXIS MEDBANK MINI CR-4HH-P 139001-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FH-P 139002-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FM-P 139000-01 BD PYXIS MEDBANK MN 200 CR-4HH-P 139020-01 BD PYXIS MEDBANK MN 500 CR-2HH-1FM-2DD-P 139018-01 BD PYXIS MEDBANK MN 500 CR-2HH-5FM-P 139019-01 BD PYXIS MEDBANK MN 500 CR-4HH-1FH-3FM-P 139021-01 BD PYXIS MEDBANK MN 500 CR-4HH-4FM-P 139022-01 BD PYXIS MEDBANK MN 500 CR-6HH-3FM-P 138973-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P 155140-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P 169-82 BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P 138975-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P 155141-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P 169-83 BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P 139073-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FH 155142-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FH 169-84 BD PYXIS MEDBANK TWR MN CR-12HH-1FH 138976-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P 155143-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P 169-85 BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P 138977-01 BD PYXIS MEDBANK TWR MN CR-14HH-P 155144-01 BD PYXIS MEDBANK TWR MN CR-14HH-P 169-86 BD PYXIS MEDBANK TWR MN CR-14HH-P 138951-01 BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM 155145-01 BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM 169-87 BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM 139072-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FH 155146-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FH 169-88 BD PYXIS MEDBANK TWR MN CR-2HH-6FH 139085-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FM 155147-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FM 169-89 BD PYXIS MEDBANK TWR MN CR-2HH-6FM 138968-01 BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P 155148-01 BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P 169-90 BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P 138964-01 BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P 155149-01 BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P 169-91 BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P 138966-01 BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P 155150-01 BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P 169-92 BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P 138967-01 BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P 155151-01 BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P 169-93 BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P 138969-01 BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P 155152-01 BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P 169-94 BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P 138965-01 BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P 155153-01 BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P 169-95 BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P 138971-01 BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P 155154-01 BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P 169-96 BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P 138972-01 BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P 155155-01 BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P 169-97 BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P 138974-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P 155156-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P 169-98 BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P 138970-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P 155157-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P 169-99 BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P

CareFusion 303, Inc.

Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.

January 8, 2025 · DeviceView details →
Class IIOngoing

139054-01 BD PYXIS MEDFLEX MN 1000 10HH-1FM 139055-01 BD PYXIS MEDFLEX MN 1000 12HH 139053-01 BD PYXIS MEDFLEX MN 1000 2HH-2FH-3FM 139041-01 BD PYXIS MEDFLEX MN 1000 2HH-2FM 139046-01 BD PYXIS MEDFLEX MN 1000 2HH-5FM 139038-01 BD PYXIS MEDFLEX MN 1000 3FM 139040-01 BD PYXIS MEDFLEX MN 1000 4HH-1FM 139049-01 BD PYXIS MEDFLEX MN 1000 4HH-4FM 139044-01 BD PYXIS MEDFLEX MN 1000 6FM 139039-01 BD PYXIS MEDFLEX MN 1000 6HH 139051-01 BD PYXIS MEDFLEX MN 1000 6HH-3FM 139164-01 BD PYXIS MEDFLEX MN 1000 8HH-2FH 139052-01 BD PYXIS MEDFLEX MN 1000 8HH-2FM 139070-01 BD PYXIS MEDFLEX MN 2000 10HH-1FM 139071-01 BD PYXIS MEDFLEX MN 2000 12HH 139061-01 BD PYXIS MEDFLEX MN 2000 2HH-2FM 139066-01 BD PYXIS MEDFLEX MN 2000 2HH-3FM-1DD 139065-01 BD PYXIS MEDFLEX MN 2000 2HH-5FM 139058-01 BD PYXIS MEDFLEX MN 2000 3FM 139060-01 BD PYXIS MEDFLEX MN 2000 4HH-1FM 139067-01 BD PYXIS MEDFLEX MN 2000 4HH-4FM 139064-01 BD PYXIS MEDFLEX MN 2000 6FM 139059-01 BD PYXIS MEDFLEX MN 2000 6HH 139068-01 BD PYXIS MEDFLEX MN 2000 6HH-3FM 139165-01 BD PYXIS MEDFLEX MN 2000 8HH-2FH 139069-01 BD PYXIS MEDFLEX MN 2000 8HH-2FM 1139-00 MEDFLEX 2.0 1119-00 MEDFLEX

CareFusion 303, Inc.

Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.

January 8, 2025 · DeviceView details →
Class IIOngoing

155288-01 BD PYXIS MEDBANK MINI 1FH-1FM 169-137 BD PYXIS MEDBANK MINI 1FH-1FM 155311-01 BD PYXIS MEDBANK MINI 1FH-2HH 138921-01 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 155159-01 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 169-101 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 139122-01 BD PYXIS MEDBANK MINI 1HH-1HM-1FM 155160-01 BD PYXIS MEDBANK MINI 1HH-1HM-1FM 169-102 BD PYXIS MEDBANK MINI 1HH-1HM-1FM 138912-01 BD PYXIS MEDBANK MINI 1HH-3HM 155161-01 BD PYXIS MEDBANK MINI 1HH-3HM 169-103 BD PYXIS MEDBANK MINI 1HH-3HM 138902-01 BD PYXIS MEDBANK MINI 2FH 169-104 BD PYXIS MEDBANK MINI 2FH 138903-01 BD PYXIS MEDBANK MINI 2FM 155163-01 BD PYXIS MEDBANK MINI 2FM 169-105 BD PYXIS MEDBANK MINI 2FM 138908-01 BD PYXIS MEDBANK MINI 2HH-1FH 169-106 BD PYXIS MEDBANK MINI 2HH-1FH 138906-01 BD PYXIS MEDBANK MINI 2HH-1FM 155165-01 BD PYXIS MEDBANK MINI 2HH-1FM 169-107 BD PYXIS MEDBANK MINI 2HH-1FM 138907-01 BD PYXIS MEDBANK MINI 2HH-2HM 155166-01 BD PYXIS MEDBANK MINI 2HH-2HM 169-108 BD PYXIS MEDBANK MINI 2HH-2HM 139131-01 BD PYXIS MEDBANK MINI 2HM-1FM 155167-01 BD PYXIS MEDBANK MINI 2HM-1FM 169-109 BD PYXIS MEDBANK MINI 2HM-1FM 139091-01 BD PYXIS MEDBANK MINI 3HH-1FG 155168-01 BD PYXIS MEDBANK MINI 3HH-1FG 169-110 BD PYXIS MEDBANK MINI 3HH-1FG 138909-01 BD PYXIS MEDBANK MINI 3HH-1HM 155169-01 BD PYXIS MEDBANK MINI 3HH-1HM 169-111 BD PYXIS MEDBANK MINI 3HH-1HM 138910-01 BD PYXIS MEDBANK MINI 4HH 155310-01 BD PYXIS MEDBANK MINI 4HH 169-112 BD PYXIS MEDBANK MINI 4HH 138915-01 BD PYXIS MEDBANK MINI 4HM 155171-01 BD PYXIS MEDBANK MINI 4HM 169-113 BD PYXIS MEDBANK MINI 4HM 1147-00 MEDBANK MINI MAIN 138943-01 BD PYXIS MEDBANK TWR MN 10HH-1FH-1FM 155081-01 BD PYXIS MEDBANK TWR MN 10HH-1FH-1FM 169-23 BD PYXIS MEDBANK TWR MN 10HH-1FH-1FM 138955-01 BD PYXIS MEDBANK TWR MN 10HH-2FH 155082-01 BD PYXIS MEDBANK TWR MN 10HH-2FH 169-24 BD PYXIS MEDBANK TWR MN 10HH-2FH 138924-01 BD PYXIS MEDBANK TWR MN 10HH-2FM 155083-01 BD PYXIS MEDBANK TWR MN 10HH-2FM 169-25 BD PYXIS MEDBANK TWR MN 10HH-2FM 138960-01 BD PYXIS MEDBANK TWR MN 12HH-1FF 155084-01 BD PYXIS MEDBANK TWR MN 12HH-1FF 169-26 BD PYXIS MEDBANK TWR MN 12HH-1FF 138961-01 BD PYXIS MEDBANK TWR MN 12HH-1FH 155085-01 BD PYXIS MEDBANK TWR MN 12HH-1FH 169-27 BD PYXIS MEDBANK TWR MN 12HH-1FH 138926-01 BD PYXIS MEDBANK TWR MN 12HH-1FM 155086-01 BD PYXIS MEDBANK TWR MN 12HH-1FM 169-28 BD PYXIS MEDBANK TWR MN 12HH-1FM 138927-01 BD PYXIS MEDBANK TWR MN 14HH 155087-01 BD PYXIS MEDBANK TWR MN 14HH 169-29 BD PYXIS MEDBANK TWR MN 14HH 155293-01 BD PYXIS MEDBANK TWR MN 1FH-10HM-1FM 169-138 BD PYXIS MEDBANK TWR MN 1FH-10HM-1FM 155303-01 BD PYXIS MEDBANK TWR MN 1FM-10HH-1FH 139082-01 BD PYXIS MEDBANK TWR MN 1HH-1HM-2FM-4FF 155088-01 BD PYXIS MEDBANK TWR MN 1HH-1HM-2FM-4FF 169-30 BD PYXIS MEDBANK TWR MN 1HH-1HM-2FM-4FF 155305-01 BD PYXIS MEDBANK TWR MN 2FH-1FM-4HH-2FM 139056-01 BD PYXIS MEDBANK TWR MN 2FH-2HM-4FM 155089-01 BD PYXIS MEDBANK TWR MN 2FH-2HM-4FM 169-31 BD PYXIS MEDBANK TWR MN 2FH-2HM-4FM 155304-01 BD PYXIS MEDBANK TWR MN 2FM-8HH-1FH 139045-01 BD PYXIS MEDBANK TWR MN 2HH-10HM-1FM 155090-01 BD PYXIS MEDBANK TWR MN 2HH-10HM-1FM 169-32 BD PYXIS MEDBANK TWR MN 2HH-10HM-1FM 138932-01 BD PYXIS MEDBANK TWR MN 2HH-1FH-5FM 155091-01 BD PYXIS MEDBANK TWR MN 2HH-1FH-5FM 169-33 BD PYXIS MEDBANK TWR MN 2HH-1FH-5FM 139084-01 BD PYXIS MEDBANK TWR MN 2HH-2FH-4FM 155092-01 BD PYXIS MEDBANK TWR MN 2HH-2FH-4FM 169-34 BD PYXIS MEDBANK TWR MN 2HH-2FH-4FM 138963-01 BD PYXIS MEDBANK TWR MN 2HH-2FM-4FF 155093-01 BD PYXIS MEDBANK TWR MN 2HH-2FM-4FF 169-35 BD PYXIS MEDBANK TWR MN 2HH-2FM-4FF 155294-01 BD PYXIS MEDBANK TWR MN 2HH-4FH-2FM 169-139 BD PYXIS MEDBANK TWR MN 2HH-4FH-2FM 138938-01 BD PYXIS MEDBANK TWR MN 2HH-4HM-4FF 155094-01 BD PYXIS MEDBANK TWR MN 2HH-4HM-4FF 169-36 BD PYXIS MEDBANK TWR MN 2HH-4HM-4FF 139125-01 BD PYXIS MEDBANK TWR MN 2HH-4HM-4FM 155095-01 BD PYXIS MEDBANK TWR MN 2HH-4HM-4FM 169-37 BD PYXIS MEDBANK TWR MN 2HH-4HM-4FM 138919-01 BD PYXIS MEDBANK TWR MN 2HH-6FM 155096-01 BD PYXIS MEDBANK TWR MN 2HH-6FM 169-38 BD PYXIS MEDBANK TWR MN 2HH-6

CareFusion 303, Inc.

Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.

January 8, 2025 · DeviceView details →
Class IIOngoing

139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI 1FH-2HH MEDPASS 169-152 BD PYXIS MEDBANK MINI 2HH-1FM MEDPASS 169-150 BD PYXIS MEDBANK MINI 4HH MEDPASS 169-140 BD PYXIS MEDBANK TWR MN 3FH-8HH MEDPASS

CareFusion 303, Inc.

Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.

January 8, 2025 · DeviceView details →
Class IIOngoing

The MSOT Acuity Echo is a Class 4 medical laser device. The MSOT Acuity is a mobile assembly of electrically-powered components intended for imaging and analysis of soft-tissue and vasculature using combined optoacoustic (photoacoustic) and ultrasound (US) imaging.

Ithera Medical Gmbh

The MSOT Acuity Echo does not include an adequate instruction for safe operation of the device. The previous version of the user manuals contained a wrong value for the Nominal Ocular Hazard Distance (NOHD).

January 8, 2025 · DeviceView details →
Class IIOngoing

(1) BD Pyxis MedStation ES, Catalog No. 323; (2) BD Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) BD Pyxis MedStation ES Tower, Catalog No. 352; (4) BD Pyxis MedStation 4000 Console, Catalog No. 309; (5) BD Pyxis MedStation 4000, Catalog No. 303; (6) BD Pyxis Anesthesia System 4000, Catalog No. 338

CareFusion 303, Inc.

Labeling is insufficient regarding delays in access to medication. The firm is strengthening the label as an additional risk mitigation.

January 8, 2025 · DeviceView details →
Class IIOngoing

stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades

Stryker Corporation

Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.

January 8, 2025 · DeviceView details →
Class IIOngoing

NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10

Zimmer, Inc.

It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.

January 6, 2025 · DeviceView details →
Class IIOngoing

NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C,D - Height 14 mm, Item Number 00-5994-022-14

Zimmer, Inc.

It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.

January 6, 2025 · DeviceView details →
Class IIOngoing

Sysmex PS-10 Sample Preparation System with software version 1.5 and 1.6., Catalog Number BQ716341. Product usage for automated pipetting, diluting, and specimen processing workstations for flow cytometric analysis.

Sysmex America, Inc.

Sysmex was made aware of a report of false results due to carry-over caused by the sporadic omission of the probe wash step during antibody pipetting on the PS-10 Sample Preparation System.

January 6, 2025 · DeviceView details →
Class IOngoing

VARIPULSE Bi-Directional Ablation Catheter REF D141201. The Field Catheter is indicated for use in catheter based cardiac electrophysiological mapping (stimulating and recording) and, when used for TRUPULSE Generator, for the treatment of drug refractory recurrent symptomatic paroxysmal atrial fibrillation. The catheter provides location information when used with the CARTO 3 System.

Biosense Webster, Inc.

Due to an observed trend of neurovascular events

January 5, 2025 · DeviceView details →
Class IIOngoing

Irix-A Integrated Lumbar Fusion System, Model Number X080-423011-08PC (Spacer Assy, 42 X 30 X 8¿, 11mm, PC (STERILE)) and Model Number X080-382819-08PC (Spacer ASSY, 38 X 28 X 8¿, 19mm, PC, (STERILE))

XTANT Medical Holdings, Inc

Certain implants in the Irix-A Lumbar Fusion System were distributed while labeled with an incorrect expiration date.

January 3, 2025 · DeviceView details →
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